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Laboratorios Ancalmo

FDA import alert and refusal historyunknown, El SalvadorFEI 3003681479

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Example subjectLaboratorios Ancalm added to Import Alert 16-129 (red list)

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As of October 26, 2026, Laboratorios Ancalmo is not on any FDA import alert in SupplierRadar's records; FDA refused 3 of its shipment lines on April 23, 2018, most often for fair packaging and labeling act (LABELING).

Data from FDA public records, last checked . Request a correction

Current status

Import alerts
Not listed
Last import refusal
Vitamin, n.e.c. · LACKS FIRM
Last warning letter
None found
Last inspection
None on record

Every FDA record for Laboratorios Ancalmo

3 records, newest first. Each line links to the FDA page it came from.

2018

  1. Import refusal
    Refused, 3 lines in one entry: Vitamin, n.e.c.LACKS FIRMNO ENGLISHLABELINGEntry 8ES-0004555-8Show 3 lines
    Source

Refusal charges, in plain English

  • LABELING3 refused lines

    Fair Packaging and Labeling Act

    The package appeared not to meet the Fair Packaging and Labeling Act because of the placement, form, or contents of a required label statement.

  • LACKS FIRM3 refused lines

    Manufacturer name and address missing

    The packaged product's label appeared not to show the name and place of business of the manufacturer, packer, or distributor.

  • NO ENGLISH3 refused lines

    Required label information not in English

    Information that must appear on the label appeared not to be given in English, or not to be repeated in every language used on the label.

Questions about Laboratorios Ancalmo

Is Laboratorios Ancalmo on an FDA import alert?
No listing for Laboratorios Ancalmo appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the El Salvador page.
Has FDA refused shipments from Laboratorios Ancalmo?
Yes. FDA refused 3 shipment lines from Laboratorios Ancalmo on April 23, 2018. The most recent, on April 23, 2018, was vitamin, n.e.c., charged as LACKS FIRM (manufacturer name and address missing).
Why did FDA refuse Laboratorios Ancalmo's shipments?
The most frequent charges are LABELING (fair packaging and labeling act, 3 lines) and LACKS FIRM (manufacturer name and address missing, 3 lines).
What is Laboratorios Ancalmo's FEI number?
Laboratorios Ancalmo's FDA Establishment Identifier (FEI) is 3003681479.

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Example subjectLaboratorios Ancalm added to Import Alert 16-129 (red list)

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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.